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Possible association of the alpha-2A-adrenergic receptor gene with response time variability in attention deficit hyperactivity disorder

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dc.contributor.authorCho, Soo-Churl-
dc.contributor.authorKim, Jae-Won-
dc.contributor.authorKim, Boong-Nyun-
dc.contributor.authorHwang, Jun-Won-
dc.contributor.authorPark, Mira-
dc.contributor.authorKim, Soon Ae-
dc.contributor.authorCho, Dae-Yeon-
dc.contributor.authorYoo, Hee-Jeong-
dc.contributor.authorChung, Un-Sun-
dc.contributor.authorSon, Jung-Woo-
dc.contributor.authorPark, Tae-Won-
dc.date.accessioned2010-04-19-
dc.date.available2010-04-19-
dc.date.issued2008-03-05-
dc.identifier.citationAm J Med Genet B Neuropsychiatr Genet. 2008 ;147B(6):957-63.en
dc.identifier.issn1552-485X (Electronic)-
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=18314873-
dc.identifier.urihttps://hdl.handle.net/10371/63308-
dc.description.abstractPrevious studies have demonstrated that the MspI and DraI polymorphisms at the alpha-2A-adrenergic receptor gene (ADRA2A) are associated with ADHD. However, few studies have been designed to ascertain the association between the ADRA2A genotypes and the performance on neurocognitive measures in ADHD. The aims of this study were to examine the association of the ADRA2A MspI and DraI polymorphisms with ADHD in Korean subjects, and to determine the relationship between the genotypes of these two polymorphisms and the candidate endophenotypes, as measured by the continuous performance test (CPT). In a case-control study, we assessed 186 ADHD probands and 150 normal controls. One hundred eight trios were studied in a family based association analysis. The transmission disequilibrium test (TDT) analysis showed preferential transmission of the C allele of the DraI polymorphism (chi(2) = 5.88, P = 0.015). In the haplotype analyses, a trend of over-transmission of haplotype C/C was observed (chi(2) = 3.80, P = 0.051). The homozygous subjects for the C allele (C/C genotype) at the DraI polymorphism showed a trend toward a higher mean T-score with respect to the response time variability profiles of the CPT than did those with the other genotypes (C/T + T/T genotypes; P = 0.042). The homozygous subjects for the G allele (G/G genotype) at the MspI polymorphism showed a tendency to have a lower mean T-score with respect to the response time variability profiles of the CPT (P = 0.068). The results of this study provide important evidence for the involvement of the ADRA2A MspI and DraI polymorphisms in the etiology of ADHD in Korean subjects. In addition, our results provide evidence for the possible role of these two polymorphisms in ADHD symptom expression, such as increased response time variability.en
dc.description.sponsorshipGrant sponsor : Seoul National University Hospital Research Fund ; Grant number:04-2006-108-0.en
dc.language.isoenen
dc.publisherWiley-Blackwellen
dc.subjectAttention Deficit Disorder with Hyperactivity/*genetics/*psychologyen
dc.subjectCase-Control Studiesen
dc.subjectChilden
dc.subjectDeoxyribonuclease HpaII/metabolismen
dc.subjectDeoxyribonucleases, Type II Site-Specific/metabolismen
dc.subjectFemaleen
dc.subjectGene Frequencyen
dc.subjectGenetic Predisposition to Diseaseen
dc.subjectGenotypeen
dc.subjectHumansen
dc.subjectKoreaen
dc.subjectLinkage Disequilibriumen
dc.subjectMaleen
dc.subjectPolymorphism, Restriction Fragment Lengthen
dc.subjectReaction Time/*geneticsen
dc.subjectReceptors, Adrenergic, alpha-2/*geneticsen
dc.titlePossible association of the alpha-2A-adrenergic receptor gene with response time variability in attention deficit hyperactivity disorderen
dc.typeArticleen
dc.contributor.AlternativeAuthor조수철-
dc.contributor.AlternativeAuthor김재철-
dc.contributor.AlternativeAuthor김붕년-
dc.contributor.AlternativeAuthor황준원-
dc.contributor.AlternativeAuthor박미라-
dc.contributor.AlternativeAuthor김순애-
dc.contributor.AlternativeAuthor조대연-
dc.contributor.AlternativeAuthor유희정-
dc.contributor.AlternativeAuthor정운선-
dc.contributor.AlternativeAuthor손정우-
dc.contributor.AlternativeAuthor박태원-
dc.identifier.doi10.1002/ajmg.b.30725-
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